Carbon corrosion mechanism on nitrogen-doped carbon support - A density functional theory study

In this work, density functional theory (DFT) calculations were used to investigate the mechanism of carbon corrosion on nitrogen-doped carbon support. Free energy diagrams were generated based on three proposed reaction pathways to evaluate corrosion mechanisms. The most energetically preferred mechanism on nitrogen-doped carbon was determined. The results show that the step of water dissociation to form (OH)-O-# was the rate-determining step for gra-G-1N (graphene doped with graphitic N) and pyrr-G-1N (graphene doped with pyrrolic N). As for graphene doped with pyridinic N, the step of (COCO)-O-#-O-# formation was critical. It was found that the control of nitrogen concentration was necessary for precisely designing optimized carbon materials. Abundance of nitrogen moieties aggravated the carbon corrosion. When the high potential was applied, specific types of graphitic N and pyridinic N were found to be favorable carbon modifications to improve carbon corrosion resistance. Moreover, the solvent effect was also investigated. The results provide theoretical insights and design guidelines to improve corrosion resistance in carbon support through material modification by inhibiting the adsorption of surface oxides (OH, O, and OOH). (C) 2021 Published by Elsevier Ltd on behalf of Hydrogen Energy Publications LLC.

Automated summary

In this work, density functional theory calculations were used to investigate the mechanism of carbon corrosion on nitrogen-doped carbon support, determining the most energetically preferred mechanism and providing theoretical insights and design guidelines for optimizing carbon materials. Abundance of nitrogen moieties aggravated carbon corrosion, while specific types of graphitic N and pyridinic N were found to improve carbon corrosion resistance. The control of nitrogen concentration was highlighted as necessary in designing optimized carbon materials.